Low-Dose vs Standard-Dose Valganciclovir for Cytomegalovirus Prophylaxis After Kidney Transplantation: A Single-Center Retrospective Analysis.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
09 Jan 2024
Historique:
received: 11 11 2023
accepted: 30 11 2023
medline: 11 1 2024
pubmed: 11 1 2024
entrez: 10 1 2024
Statut: aheadofprint

Résumé

Prophylactic administration of valganciclovir (VG) is an accepted method for the prevention of cytomegalovirus (CMV) infection after kidney transplantation (KTx). The standard dosage of oral VG is 900 mg/day, adjusted to renal function. There is growing evidence that low-dose 450 mg/day VG might be safe and effective. We compared low-dose vs standard-dose prophylaxis after KTx in a single-center follow-up study. Data from 603 renal transplantations at a single center were retrospectively analyzed (2011-2014, 12-month follow-up). Recipients with donor IgG positive-recipient IgG positive (D+/R+), (D+/R-), and (D-/R+) CMV serostatus were routinely treated with 450 mg/day VG for 3 months. Based on the same prophylactic dose, patients could be categorized into two groups according to their postoperative renal function: those receiving standard-dose VG due to a lower estimated glomerular filtration rate (eGFR) (average eGFR<60 mL/min/1.73 m Estimated glomerular filtration rate-based VG serum alterations significantly affected the risk of CMV infection with a higher incidence in higher VG levels (standard-dose: 357 patients, CMV: 33 cases (9.2 %); low-dose: 246 patients, CMV: 10 cases (4.1%). The occurrence of known risk factors: serologic risk distribution and rate of induction therapy were not statistically different between the 2 groups. Treatment of an acute rejection episode influenced the infection rate significantly in the standard-dose group. As a side effect of prophylaxis, leucopenia (<3G/L) was 2.46 times higher in standard-dose vs low-dose group. Low-dose VG administration is safe and non-inferior to the standard dose in the prophylaxis of CMV infection after KTx.

Sections du résumé

BACKGROUND BACKGROUND
Prophylactic administration of valganciclovir (VG) is an accepted method for the prevention of cytomegalovirus (CMV) infection after kidney transplantation (KTx). The standard dosage of oral VG is 900 mg/day, adjusted to renal function. There is growing evidence that low-dose 450 mg/day VG might be safe and effective. We compared low-dose vs standard-dose prophylaxis after KTx in a single-center follow-up study.
METHODS METHODS
Data from 603 renal transplantations at a single center were retrospectively analyzed (2011-2014, 12-month follow-up). Recipients with donor IgG positive-recipient IgG positive (D+/R+), (D+/R-), and (D-/R+) CMV serostatus were routinely treated with 450 mg/day VG for 3 months. Based on the same prophylactic dose, patients could be categorized into two groups according to their postoperative renal function: those receiving standard-dose VG due to a lower estimated glomerular filtration rate (eGFR) (average eGFR<60 mL/min/1.73 m
RESULTS RESULTS
Estimated glomerular filtration rate-based VG serum alterations significantly affected the risk of CMV infection with a higher incidence in higher VG levels (standard-dose: 357 patients, CMV: 33 cases (9.2 %); low-dose: 246 patients, CMV: 10 cases (4.1%). The occurrence of known risk factors: serologic risk distribution and rate of induction therapy were not statistically different between the 2 groups. Treatment of an acute rejection episode influenced the infection rate significantly in the standard-dose group. As a side effect of prophylaxis, leucopenia (<3G/L) was 2.46 times higher in standard-dose vs low-dose group.
CONCLUSION CONCLUSIONS
Low-dose VG administration is safe and non-inferior to the standard dose in the prophylaxis of CMV infection after KTx.

Identifiants

pubmed: 38199858
pii: S0041-1345(23)00783-2
doi: 10.1016/j.transproceed.2023.11.021
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Katalin Farkas (K)

Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.

Marina Varga (M)

Department of Laboratory Medicine, Semmelweis University, Faculty of Medicine, Budapest, Hungary.

Izabella Dinnyes (I)

Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.

Lili Rem (L)

Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.

Gabor Telkes (G)

Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.

Laszlo Wagner (L)

Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.

Adam Remport (A)

Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.

Laszlo Piros (L)

Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.

Attila Szijarto (A)

Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.

Gergely Huszty (G)

Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary. Electronic address: ghuszty@gmail.com.

Classifications MeSH